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Members of the fragile X gene family exhibit genetic and phenotypic interaction in mammals

โœ Scribed by D.L. Nelson; J. Zhang; O.Sofola; Z. Fang; K. Kaasik; C.C. Lee; R. Willemsen; E. Klann; R. Jackson; J. Botas; B.A. Oostra


Book ID
116551453
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
40 KB
Volume
24
Category
Article
ISSN
0736-5748

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Deletion of 8.5 Mb, including theFMR1 ge
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A four-year-old boy with severe psychomotor retardation, facial appearance consistent with the fragile X syndrome, hypotonia, and overgrowth was found to have a deletion including the fragile X gene (FMR1). The breakpoints of the deletion were established between CDR1 and sWXD2905 (approximately 200